Evidence map›Paper›PMID 27378515›Full record

ArticleEuropean journal of immunology2016

IL-10 differentially controls the infiltration of inflammatory macrophages and antigen-presenting cells during inflammation.

Chia-Te Liao, Marcela Rosas, Luke C Davies, Peter J Giles, Victoria J Tyrrell, Valerie B O'Donnell, Nicholas Topley, Ian R Humphreys, Donald J Fraser, Simon A Jones and 1 more

Open access · hybridAbstract read
In one paragraph

Article in European journal of immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.7field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  4. Review
  5. Article
  6. CD11c identifies microbiota and EGR2-dependent MHCIIEuropean journal of immunology · 2022
    Article
  7. The Relationship between Cancer and Paraoxonase 1.Antioxidants (Basel, Switzerland) · 2022
    Review
  8. Article
  9. Article
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  15. Review
  16. Journal of immunology (Baltimore, Md. : 1950) · 2018
    Article
  17. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Chia-Te LiaoDivision of Infection and Immunity, Cardiff University School of Medicine, Heath Park, Cardiff, UK.
Marcela RosasDivision of Infection and Immunity, Cardiff University School of Medicine, Heath Park, Cardiff, UK.
Luke C DaviesDivision of Infection and Immunity, Cardiff University School of Medicine, Heath Park, Cardiff, UK.
Peter J GilesCentral Biotechnology Services, Cardiff University School of Medicine, Heath Park, Cardiff, UK.
Victoria J TyrrellDivision of Infection and Immunity, Cardiff University School of Medicine, Heath Park, Cardiff, UK.
Valerie B O'DonnellDivision of Infection and Immunity, Cardiff University School of Medicine, Heath Park, Cardiff, UK.
Nicholas TopleySystems Immunity University Research Institute, Cardiff University School of Medicine, Heath Park, Cardiff, UK.
Ian R HumphreysDivision of Infection and Immunity, Cardiff University School of Medicine, Heath Park, Cardiff, UK.
Donald J FraserDivision of Infection and Immunity, Cardiff University School of Medicine, Heath Park, Cardiff, UK.
Simon A JonesDivision of Infection and Immunity, Cardiff University School of Medicine, Heath Park, Cardiff, UK.
Philip R TaylorDivision of Infection and Immunity, Cardiff University School of Medicine, Heath Park, Cardiff, UK. TaylorPR@cf.ac.uk.
Cardiff University · GB

Funding

Medical Research Council MR/J002151/1Medical Research Council MR/K02003X/1Versus Arthritis 20770Wellcome Trust 094143/Z/10/ZWellcome Trust WT107964MA
6 · The paper itself

Abstract

The inflammatory activation and recruitment of defined myeloid populations is essential for controlling the bridge between innate and adaptive immunity and shaping the immune response to microbial challenge. However, these cells exhibit significant functional heterogeneity and the inflammatory signals that differentially influence their effector characteristics are poorly characterized. In this study, we defined the phenotype of discrete subsets of effective antigen-presenting cells (APCs) in the peritoneal cavity during peritonitis. When the functional properties of these cells were compared to inflammatory monocyte-derived macrophages we noted differential responses to the immune-modulatory cytokine IL-10. In contrast to the suppressive actions of IL-10 on inflammatory macrophages, the recruitment of APCs was relatively refractory and we found no evidence for selective inhibition of APC differentiation. This differential response of myeloid cell subsets to IL-10 may thus have limited impact on development of potentially tissue-damaging adaptive immune responses, while restricting the magnitude of the inflammatory response. These findings may have clinical relevance in the context of peritoneal dialysis patients, where recurrent infections are associated with immune-mediated membrane dysfunction, treatment failure, and increased morbidity.

Indexed as

AnimalsAntigen PresentationAntigen-Presenting CellsBiomarkersCells, CulturedDendritic CellsDisease Models, AnimalImmunomodulationImmunophenotypingInflammationInterleukin-10MacrophagesMiceMice, KnockoutPeritonitisPhenotypeBiomarkersInterleukin-10Receptors, CCR2Antigen presentingAntigen processingDendritic cellsFate-mappingInflammationMacrophagesMonocytes

Identifiers

PMID27378515
PMCPMC5026061
OpenAlexW2460906442

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.